Zobrazeno 1 - 10
of 263
pro vyhledávání: '"Pujol-Moix, N."'
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Pecci, A, Klersy, C, Gresele, P, Lee, K, De Rocco, D, Bozzi, V, Russo, G, Heller, Pg, Loffredo, G, Ballmaier, M, Fabris, F, Beggiato, E, Kahr, Wha, Pujol-Moix, N, Platokouki, H, Matthijs, G, Noris, P, Yerram, P, Hermans, C, Batzios, S, De Groot, M, Zieger, B, De Candia, E, Fraticelli, V, Kersseboom, R, Piccoli, Gb, Zimmermann, S, Zaninetti, C, Nicchia, E, Baronci, C, Seri, M, Knight, Pj, Balduini, Cl, Savoia, A, Van Geet, C, Geber, B, Economou, M, Fierro, T, Glembotsky, Ac, Vianello, F, Guthner, C.
Publikováno v:
Human Mutation, 35(2), 236-247. Wiley
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
HUMAN MUTATION
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
HUMAN MUTATION
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
MYH9-related disease (MYH9-RD) is a rare autosomal-dominant disorder caused by mutations in the gene for nonmuscle myosin heavy chain IIA (NMMHC-IIA). MYH9-RD is characterized by a considerable variability in clinical evolution: patients present at b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0b3202308793ba3d6d45b4fe01ee6e8
https://research.rug.nl/en/publications/8f687127-8140-4108-abe8-7c14ccda866a
https://research.rug.nl/en/publications/8f687127-8140-4108-abe8-7c14ccda866a
Autor:
Noris, P., Civaschi, E., Catherine Klersy, Melazzini, F., Pujol-Moix, N., Santoro, C., Cattaneo, M., Lavenu-Bombled, C., Bury, L., Minuz, P., Nurden, P., Cid-Haro, A. R., Cuker, A., Latger-Cannard, V., Favier, R., Nichele, I., Balduini, C. L.
Publikováno v:
Publons
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::e2abf07f0112ca9693b17d5a2938767a
http://hdl.handle.net/11573/988434
http://hdl.handle.net/11573/988434
Autor:
Civaschi E, Klersy C, Melazzini F, Pujol-Moix N, Santoro C, Cattaneo M, Lavenu-Bombled C, Bury L, Minuz P, Nurden P, Ar, Cid, Cuker A, Latger-Cannard V, Favier R, Nichele I, Patrizia Noris, European Haematology Association - Scientific Working Group on Thrombocytopenias and Platelet Function Disorders
Publikováno v:
BRITISH JOURNAL OF HAEMATOLOGY
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Europe PubMed Central
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Europe PubMed Central
This study evaluated 65 pregnancies in 34 women with five different inherited platelet function disorders. Gestation was similar to that of the general population. Severe bleeds requiring blood transfusions were observed in 50% of deliveries in Glanz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::c2b31aa3ebfce202913b36549a20391f
https://fundanet.iislafe.san.gva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=2035
https://fundanet.iislafe.san.gva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=2035
Autor:
De Candia, E., Bottega, Roberta, Pecci, A., Pujol Moix, N., Heller, P., Noris, P., DE ROCCO, Daniela, Podda, G. M., Balduini, C. L., Savoia, Anna
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::8532a750443ffdc3d8b15a86e608e405
https://hdl.handle.net/11368/2625642
https://hdl.handle.net/11368/2625642
Autor:
García-Dabrio M.C., Pujol-Moix N., Martinez-Perez A., Fontcuberta J., Souto J.C., Soria J.M., Nomdedéu J.F.
Publikováno v:
ACTA HAEMATOLOGICA
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Introduction: Flow cytometry analysis of lymphocyte subsets in peripheral blood is a common technique in diagnostic laboratories. Abnormal values have been identified in prevalent infections, autoimmune disorders and neoplastic diseases. Reference ra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::c0c05181b3152e6dbc209aa59c283da5
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84860190478&doi=10.1159/000337051&partnerID=40&md5=d7298a14f671d256fe8fdb22c9f86bed
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84860190478&doi=10.1159/000337051&partnerID=40&md5=d7298a14f671d256fe8fdb22c9f86bed
Publikováno v:
Dipòsit Digital de la UB
Universidad de Barcelona
Scopus-Elsevier
Universidad de Barcelona
Scopus-Elsevier
Background and objectives: storage pool diseases (SPD) are heterogeneous disorders associated with an abnormal presence of intraplatelet granules, which cause mild to moderate bleeding diathesis. We investigated signaling through tyrosine phosphoryla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::c0f2c94168c304498389ec867e2f01c8
http://hdl.handle.net/2445/172732
http://hdl.handle.net/2445/172732
Publikováno v:
Scopus-Elsevier
Europe PubMed Central
Europe PubMed Central
Thrombocytopenia in chronic liver diseases has traditionally been considered a consequence of platelet pooling and destruction in spleen. We tried to evaluate the influence of thrombopoietin, the physiological regulator of thrombopoiesis, on the orig
Publikováno v:
In Journal of Thrombosis and Haemostasis February 2009 7(2):361-363
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.